ClinVar Miner

List of variants in gene WRN reported by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 35
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000553.6(WRN):c.1953C>T (p.Gly651=) rs11574263 0.00627
NM_000553.6(WRN):c.3875C>A (p.Ser1292Tyr) rs142614369 0.00132
NM_000553.6(WRN):c.1105C>T (p.Arg369Ter) rs17847577 0.00033
NM_000553.6(WRN):c.130C>G (p.Leu44Val) rs139775895 0.00031
NM_000553.6(WRN):c.3259A>G (p.Lys1087Glu) rs374154973 0.00028
NM_000553.6(WRN):c.2986G>A (p.Asp996Asn) rs138379977 0.00026
NM_000553.6(WRN):c.1382C>T (p.Thr461Met) rs371602600 0.00020
NM_000553.6(WRN):c.4127C>T (p.Pro1376Leu) rs146055899 0.00010
NM_000553.6(WRN):c.3623A>G (p.Lys1208Arg) rs529421538 0.00009
NM_000553.6(WRN):c.1840A>G (p.Ile614Val) rs577000913 0.00008
NM_000553.6(WRN):c.3819+5G>C rs770289356 0.00008
NM_000553.6(WRN):c.1388A>G (p.Tyr463Cys) rs1339450958 0.00004
NM_000553.6(WRN):c.2263G>A (p.Val755Ile) rs769448856 0.00004
NM_000553.6(WRN):c.3284C>T (p.Pro1095Leu) rs746470648 0.00004
NM_000553.6(WRN):c.3778G>A (p.Ala1260Thr) rs201107091 0.00004
NM_000553.6(WRN):c.674G>A (p.Arg225Gln) rs62506077 0.00004
NM_000553.6(WRN):c.1652C>T (p.Pro551Leu) rs781107893 0.00003
NM_000553.6(WRN):c.2098G>A (p.Val700Ile) rs1038838933 0.00003
NM_000553.6(WRN):c.2978G>A (p.Arg993His) rs370713742 0.00003
NM_000553.6(WRN):c.4001T>G (p.Leu1334Arg) rs200403732 0.00003
NM_000553.6(WRN):c.3913C>T (p.Arg1305Ter) rs121908446 0.00002
NM_000553.6(WRN):c.1351-1G>A rs1170732591 0.00001
NM_000553.6(WRN):c.1457C>T (p.Thr486Met) rs761328537 0.00001
NM_000553.6(WRN):c.3384-1G>A rs776963381 0.00001
NM_000553.6(WRN):c.655-20A>G rs1056118121 0.00001
NM_000553.6(WRN):c.725-3del rs778493200 0.00001
NM_000553.6(WRN):c.1898+2T>G rs772319506
NM_000553.6(WRN):c.202G>T (p.Asp68Tyr) rs2130005767
NM_000553.6(WRN):c.3209_3211delinsTTT (p.Cys1070_Pro1071delinsPheSer) rs878854138
NM_000553.6(WRN):c.3244del (p.Val1082fs) rs745905108
NM_000553.6(WRN):c.3309+1G>T rs1281075870
NM_000553.6(WRN):c.3590del (p.Asn1197fs) rs281865160
NM_000553.6(WRN):c.3814C>T (p.Pro1272Ser) rs776989868
NM_000553.6(WRN):c.4011G>A (p.Met1337Ile) rs544317387
NM_000553.6(WRN):c.836G>C (p.Arg279Pro) rs768400363

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.